A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526174



Internal ID15106781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28254835..28312149hg38UCSC Ensembl
Innerchr16:28266156..28323470hg19UCSC Ensembl
Innerchr16:28173657..28230971hg18UCSC Ensembl
Innerchr16:28173657..28230971hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3857315
hg1957315
hg1857315
hg1757315
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702435
Samples
Known GenesSBK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526174
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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